Water → 6-Chloro-4-(2-propen-1-yl)-1,2,4-benzotriazin-3(4H)-one 1-oxide

6-Chloro-1,2,4-benzotriazin-3(4H)-one 1-oxide (700 mg, 3.544 mmol) was suspended in dry DMF (20 ml) under argon at rt, and the stirred suspension was treated with K2CO3 (1.614 mg, 11.695 mmol) and allyl iodide (0.43 ml, 4.607 mmol). It was then stirred at rt for 2 h before addition of further allyl iodide (0.86 ml, 9.214 mmol) and then the reaction was heated at 60° C. for 1 h before addition of water (100 ml). The mixture was then extracted with DCM (3×200 ml). The combined organic extracts were dried over anhydrous magnesium sulphate, filtered and evaporated under reduced pressure to give a yellow solid which was purified by column chromatography on silica with a 0-5% MeOH in DCM gradient to give the desired product as a light brown solid (472 mg, 56%).

1. extractionThe mixture was then extracted with DCM (3×200 ml)
2. dry with materialThe combined organic extracts were dried over anhydrous magnesium sulphate
3. filtrationfiltered
4. customevaporated under reduced pressure
5. customto give a yellow solid which
6. customwas purified by column chromatography on silica with a 0-5% MeOH in DCM gradient

ORD-Eintrag

ord-2a2f8a9b0d294790b3483da4a9556be4

Quelldatensatz

uspto-grants-2011_12

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US08071592B2